OBO ID: DOID:0080548 |
Term Name: | Noonan syndrome with multiple lentigines 1 | Search Ontology: | |
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Definition: | A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the PTPN11 gene on chromosome 12q24. https://ghr.nlm.nih.gov/condition/noonan-syndrome-with-multiple-lentigines#genes | ||
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Ontology: | Human Disease ( DOID:0080548 ) |
OTHER Noonan syndrome with multiple lentigines 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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